D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter

FDA 510(k) K242254 · Dk Medical Technology Co., Ltd.

Substantially Equivalent

510(k) numberK242254

Submission

Device name
D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter
Applicant
Dk Medical Technology Co., Ltd.
Jiangsu, CN
Received
July 31, 2024
Decision date
April 21, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
PNO – Catheter, Percutaneous, Cutting/Scoring
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1250
Specialty
Cardiovascular

To reduce vascular stenosis by dilatation and apposition of the cutting/scoring surfaces to the stenotic material

Other 510(k)s with product code PNO

510(k)DeviceApplicantDecision
K260012UltraScore™ Focused Force PTA BalloonPNO · Special Bard Peripheral Vascular, Inc.02/04/2026SE
K243944Aperta NSE PTA Balloon Dilatation CatheterPNO · Traditional Goodman Co., Ltd.04/22/2025SE
K241478Tri-Wedge PTA Scoring Balloon Dilatation CatheterPNO · Traditional Brosmed Medical Co., Ltd.10/22/2024SE
K232258XO Constrain™ Percutaneous Transluminal Angioplasty Constraining CatheterPNO · Traditional Transit Scientific, LLC06/17/2024SE
K232013Aperta NSE PTA Balloon Dilatation Catheter (AW18-05040040/AA18-05040040…PNO · Traditional Goodman Co., Ltd.03/28/2024SE
K232207D·Kutting™ PTA Scoring Balloon Dilatation CatheterPNO · Traditional Dk Medical Technology Co., Ltd.03/07/2024SE
K221986XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP CatheterPNO · Special Transit Scientific, LLC10/18/2022SE
K220704Serranator PTA Serration Balloon CatheterPNO · Traditional Cagent Vascular, LLC05/04/2022SE
K213728Serranator PTA Serration Balloon CatheterPNO · Special Cagent Vascular, LLC12/15/2021SE
K203437Serranator PTA Serration Balloon CatheterPNO · Special Cagent Vascular, LLC12/22/2020SE

More from Cagent Vascular, LLC

510(k)DeviceDecision
K232207D·Kutting™ PTA Scoring Balloon Dilatation CatheterPNO · Traditional 03/07/2024SE
K214009D·Kaptain PTA High Pressure Balloon Dilatation CatheterLIT · Traditional 04/05/2023SE

Questions and answers

When was D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter cleared by the FDA?

D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter (K242254) received a 510(k) decision of Substantially Equivalent on April 21, 2025, 264 days after the submission was received.

What is the product code of K242254?

The FDA product code is PNO – Catheter, Percutaneous, Cutting/Scoring, a Class II (moderate risk) device regulated under 21 CFR 870.1250.